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H Scheffer

Showing results (41-50 of 154) with videos related to

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European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|July 1, 1994
Tissue kallikrein activity and kinin release in human endothelial cellsK Graf, M Gräfe, W Auch-Schwelk, et al.
Human Genetics|May 1, 1995
Number and sex of offspring of delta F508 carriers outside cystic fibrosis familiesH G de Vries, J M Collée, W P Meeuwsen, et al.
Nucleic Acids Research|January 12, 1987
A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22]A M Bowcock, H Scheffer, J M Hebert, et al.
Prenatal Diagnosis|September 1, 1992
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reactionM De Boer, B G Bolscher, R H Sijmons, et al.
The American Journal of Gastroenterology|August 10, 2005
Impaired bolus transit across the esophagogastric junction in postfundoplication dysphagiaR C H Scheffer, M Samsom, A Haverkamp, et al.
Human Mutation|January 1, 1996
Comprehensive and accurate mutation scanning of the CFTR gene by two-dimensional DNA electrophoresisY Wu, R M Hofstra, H Scheffer, et al.
The British Journal of Surgery|September 24, 2004
Long-term effect of fundoplication on motility of the oesophagus and oesophagogastric junctionR C H Scheffer, M Samsom, T G Frakking, et al.
Cancer Research|December 1, 1992
Analysis of a metastasizing testicular mixed gonadal stromal tumor with osteosarcoma components suggests that a malignant tumor with the histology of osteosarcoma may develop without primary involvement of RB1 and TP53P T Reuvekamp, R P Stulp, H Schraffordt Koops, et al.
Human Genetics|December 1, 1987
Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson diseaseH Scheffer, I P Kema, I Kondo, et al.
American Journal of Human Genetics|October 1, 1995
Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophyJ M Cobben, G van der Steege, P Grootscholten, et al.
Pageof 16

Showing results (41-50 of 154) with videos related to

Sort By:
Pageof 16
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|July 1, 1994
Tissue kallikrein activity and kinin release in human endothelial cellsK Graf, M Gräfe, W Auch-Schwelk, et al.
Human Genetics|May 1, 1995
Number and sex of offspring of delta F508 carriers outside cystic fibrosis familiesH G de Vries, J M Collée, W P Meeuwsen, et al.
Nucleic Acids Research|January 12, 1987
A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22]A M Bowcock, H Scheffer, J M Hebert, et al.
Prenatal Diagnosis|September 1, 1992
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reactionM De Boer, B G Bolscher, R H Sijmons, et al.
The American Journal of Gastroenterology|August 10, 2005
Impaired bolus transit across the esophagogastric junction in postfundoplication dysphagiaR C H Scheffer, M Samsom, A Haverkamp, et al.
Human Mutation|January 1, 1996
Comprehensive and accurate mutation scanning of the CFTR gene by two-dimensional DNA electrophoresisY Wu, R M Hofstra, H Scheffer, et al.
The British Journal of Surgery|September 24, 2004
Long-term effect of fundoplication on motility of the oesophagus and oesophagogastric junctionR C H Scheffer, M Samsom, T G Frakking, et al.
Cancer Research|December 1, 1992
Analysis of a metastasizing testicular mixed gonadal stromal tumor with osteosarcoma components suggests that a malignant tumor with the histology of osteosarcoma may develop without primary involvement of RB1 and TP53P T Reuvekamp, R P Stulp, H Schraffordt Koops, et al.
Human Genetics|December 1, 1987
Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson diseaseH Scheffer, I P Kema, I Kondo, et al.
American Journal of Human Genetics|October 1, 1995
Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophyJ M Cobben, G van der Steege, P Grootscholten, et al.
Pageof 16